MTS156-IFU01-EN-230809-MC
Version 1.0
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MediCapture® MTS156 Instructions for Use – English
Residual Risks
Important Safety Instructions to avoid residual risks.
1. Read all of these instructions and Instructions for Use of the host device.
2. Keep these instructions.
3. Heed all warnings in these instructions.
4. Follow all of these instructions.
5. Do not misuse this apparatus.
6. Make sure that your video source is directly connected to the main monitor via primary safety wiring.
7. Clean the device regularly with a soft cloth moistened with ethanol 75%. Follow the disinfectant
manufacturer’s instructions!
▪ Before disinfection, the device must be cleaned to remove debris. Removal of debris can be accomplished by using a
dry, clean cloth.
• Disinfectant/sterilant: U.S. Environmental Protection Agency (EPA) approved
▪ Ethyl Alcohol, 75%
▪ Pour approximately 5ml of ethyl alcohol on a sterile cotton swab.
▪ Swipe the surface area of the device being careful not to come in contact with any of electrical connections on the back.
IMPORTANT! Make sure that no humidity enters the device. Do not use any cleaning agents, scouring agents
or solvents on this device.
8. Do not install near any heat source such as radiators, heat registers, stoves or other apparatus that produces heat.
9. Only use attachments/accessories specied by the manufacturer.
10. This device is only use in mounting status as a FIX type equipment. According to US deviation in 60601-1, FIX type equipment
shall be Class I type to comply with NEC requirement.
All FIXED medical electrical (ME) EQUIPMENT and PERMANENTLY INSTALLED medical electrical (ME) EQUIPMENT shall
be CLASS I medical electrical (ME) EQUIPMENT.
11. When using the VESA mounting option, make sure that the screws are the correct length. Screws that are too long may
damage the product, and screws that are too short may compromise stability.
See chapter Back Panel – VESA Mount.
12. Ensure that the mount is installed by qualied personnel and follow the instructions for the VESA mount (not supplied by
MediCapture).
The ACCOMPANYING DOCUMENTS shall contain instructions on attachment of structures to a oor, wall, ceiling, etc.
making adequate allowances for quality of the materials used to make the connection and shall list the required
materials. Additionally, there shall be advice on checking the adequacy of the surface of the structure to which the
parts will be attached.
13. Unplug this apparatus during lightning storms or when unused for long periods of time
Disconnection Method: Disconnect the USB cable.
14. Do not place vessels containing water or other liquids (such as vases, etc.) on top of the apparatus. Do not splash water on
top of the apparatus.
15. Refer all servicing to qualied service personnel. Servicing is required when the apparatus has been damaged in any way,
such as when a plug has been damaged, liquid has been spilled on the apparatus, objects have fallen into the apparatus, and
the apparatus has been exposed to rain or moisture, or does not operate normally, or has been dropped.
16. In case of breakdown, Service Equipment is performed by qualied personnel only, where qualied personnel refers to the
person with proper education or training assigned by the hospital, medical institution or authorized distributor.
17. This device does not have any serviceable parts. Repairs are carried out exclusively in MediCapture
service centers.
18. This device shall be used with a Class 1 type host device.
19. This equipment complies with the IEC 60601 safety standard only when connected to equipment that complies with the
IEC 60601-1 standard or applicable ISO or IEC standards. Anyone who connects equipment to the signal input is conguring
a medical system and is therefore responsible that the system complies with the requirements of medical system standard
IEC 60601-1. Equipment not complying with UL/EN/IEC 60601-1 shall be kept outside the patient environment, as dened on
the systems standard.
